aspartic acid has been researched along with Deficiency, Mental in 40 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 25 (62.50) | 18.7374 |
1990's | 5 (12.50) | 18.2507 |
2000's | 7 (17.50) | 29.6817 |
2010's | 1 (2.50) | 24.3611 |
2020's | 2 (5.00) | 2.80 |
Authors | Studies |
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Barsotti, N; Borello, U; Carotenuto, M; D'Argenio, V; De Rosa, A; Di Maio, A; Errico, F; Galbusera, A; Garofalo, M; Gozzi, A; Heresco-Levy, U; Leggiero, E; Lombardo, B; Malatesta, P; Mandarino, A; Migliarini, S; Napolitano, F; Nunziato, M; Nuzzo, T; Pagani, M; Pasqualetti, M; Pastore, L; Ranieri, A; Salvatore, F; Terrile, M; Usiello, A; Vitale, A | 1 |
Chang, MC; Kilberg, MS; Malut, VR; Merritt, ME; Pierre, GL; Staklinski, SJ | 1 |
Bellini, T; Morana, G; Pezzella, M; Rossi, A; Striano, P | 1 |
Alkan, A; Aslan, M; Kutlu, R; Orkan, I; Sigirci, A; Yakinci, C | 1 |
Afridi, SK; Chih, B; Clark, L; Scheiffele, P | 1 |
Bodensteiner, JB; Johnsen, SD; Kerrigan, JF | 1 |
Akinci, A; Alkan, A; Firat, AK; Güngör, S; Tabel, Y | 1 |
Becker, C; Gehler, J; Hartmann, J; Sewell, AC; Spranger, J | 1 |
Harada, M; Hashimoto, T; Kuroda, Y; Miyazaki, M; Miyoshi, H; Tanouchi, M; Tayama, M; Yoneda, Y; Yoshimoto, T | 2 |
Brockmann, K; Frahm, J; Hanefeld, F; Kruse, B; Pouwels, PJ; Wick, M; Wilken, B | 1 |
Ahmad, A; Artigas-Lopez, M; Kahler, SG; Kishnani, PS; Millington, DS; Pappu, AS; Steiner, R; Van Hove, JL | 1 |
Jakobs, C; Maaswinkel-Mooij, P; Onkenhout, W; Peeters, EA; Pouwels, PJ; Stöckler-Ipsiroglu, S; van der Knaap, MS; Verhoeven, NM | 1 |
Critchley, HD; Daly, EM; Glover, A; Murphy, DG; Robertson, DM; Russell, A; Simmons, A; van Amelsvoort, T | 1 |
Braun, K; Gruss, M | 1 |
Borud, O; Lie, SO; Strömme, JH; Torp, KH | 1 |
Borud, O; Dahl, T; Torp, KH | 1 |
Konttinen, A; Palo, J; Savolainen, H; Somer, H | 1 |
Bardet, J; de Blois, MC; Kamoun, P; Lejeune, J; Parvy, P; Peeters, M; Rabier, D; Rethoré, MO | 1 |
Rao, DN; Reddy, PP; Swarna, M | 1 |
Baryshnikov, VA; Ermolina, LA; Turova, NF | 1 |
Bollgren, I; Hagenfeldt, L; Venizelos, N | 1 |
Jenner, FA; Merskey, H; Pollitt, RJ | 1 |
Autio, S; Järvinen, H; Visakorpi, JK | 1 |
Gaffuri, G | 1 |
Galewicz, A; Gorska, D; Rodo, M; Zaremba, J | 1 |
Autio, S | 1 |
Pollitt, RJ; Pretty, KM | 1 |
de Groot, CJ; Hommes, FA | 1 |
Jenner, FA | 1 |
Autio, S; Palo, J | 2 |
Antich, J; Ferre, C; Sabater, J | 1 |
Hessing, J; Schweikhardt, F | 1 |
Mattsson, K; Palo, J | 1 |
Greer, M; Sprinkle, T; Williams, CM | 1 |
Hirsch, W; Mex, A; Vogel, F | 1 |
Jenner, FA; Pollitt, RJ | 1 |
Dolan, TF; Nelligan, DJ; Shih, VE; Solitare, GB | 1 |
1 review(s) available for aspartic acid and Deficiency, Mental
Article | Year |
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Aspartylglycosaminuria. Analysis of thirty-four patients.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Birth Order; Birth Weight; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diagnosis, Differential; Electrocardiography; Electroencephalography; Female; Finland; Geography; Glucosamine; Humans; Infant; Intellectual Disability; Intelligence Tests; Life Expectancy; Male; Pedigree; Socioeconomic Factors | 1972 |
39 other study(ies) available for aspartic acid and Deficiency, Mental
Article | Year |
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D-aspartate oxidase gene duplication induces social recognition memory deficit in mice and intellectual disabilities in humans.
Topics: Adult; Animals; Aspartic Acid; Autism Spectrum Disorder; D-Aspartate Oxidase; D-Aspartic Acid; Gene Duplication; Humans; Intellectual Disability; Memory Disorders; Mice; Oxidoreductases; Receptors, N-Methyl-D-Aspartate | 2022 |
Metabolomic Profiling of Asparagine Deprivation in Asparagine Synthetase Deficiency Patient-Derived Cells.
Topics: Amino Acid Metabolism, Inborn Errors; Asparagine; Aspartate-Ammonia Ligase; Aspartic Acid; Atrophy; Humans; Intellectual Disability; Microcephaly | 2023 |
Rhombencephalosynapsis in a patient with mental retardation, epilepsy, and dysmorphisms.
Topics: Adolescent; Aspartic Acid; Body Dysmorphic Disorders; Creatine; Epilepsy; Humans; Intellectual Disability; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Rhombencephalon | 2011 |
Pyridoxine-dependent seizures: magnetic resonance spectroscopy findings.
Topics: Aspartic Acid; Brain Damage, Chronic; Child; Choline; Consanguinity; Creatine; Diagnosis, Differential; Epilepsy, Generalized; Female; Follow-Up Studies; Frontal Lobe; gamma-Aminobutyric Acid; Glutamic Acid; Humans; Inositol; Intellectual Disability; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Occipital Lobe; Parietal Lobe; Phosphocreatine; Pyridoxine; Reference Values; Vitamin B 6 Deficiency | 2004 |
Disorder-associated mutations lead to functional inactivation of neuroligins.
Topics: Animals; Arginine; Aspartic Acid; Autistic Disorder; Carrier Proteins; Cell Adhesion Molecules, Neuronal; Chlorocebus aethiops; COS Cells; Genetic Predisposition to Disease; Hippocampus; Humans; Intellectual Disability; Membrane Proteins; Mutation, Missense; Nerve Tissue Proteins; Neurons; Point Mutation; Protein Transport | 2004 |
Leukoencephalopathy with bilateral anterior temporal lobe cysts.
Topics: Adolescent; Aspartic Acid; Brain Neoplasms; Central Nervous System Cysts; Child; Child, Preschool; Female; Follow-Up Studies; Humans; Inositol; Intellectual Disability; Male; Psychomotor Disorders; Retrospective Studies; Temporal Lobe | 2006 |
Neuroimaging findings in hyperargininemia.
Topics: Arginine; Aspartic Acid; Atrophy; Basal Ganglia Cerebrovascular Disease; Brain Diseases; Cerebellum; Cerebral Cortex; Child, Preschool; Choline; Consanguinity; Creatine; Dominance, Cerebral; Energy Metabolism; Humans; Hyperargininemia; Image Processing, Computer-Assisted; Intellectual Disability; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Nerve Fibers, Myelinated; Putamen | 2008 |
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family.
Topics: Abnormalities, Multiple; Acetylglucosamine; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Fabry Disease; Facial Bones; Female; Glucosamine; Humans; Intellectual Disability; Italy; Male; Pedigree; Skull | 1981 |
Reduced N-acetylaspartate in the brain observed on in vivo proton magnetic resonance spectroscopy in patients with mental retardation.
Topics: Adolescent; Aspartic Acid; Brain; Brain Chemistry; Child; Child, Preschool; Choline; Creatine; Female; Humans; Intellectual Disability; Intelligence; Magnetic Resonance Spectroscopy; Male | 1995 |
Differences in brain metabolites between patients with autism and mental retardation as detected by in vivo localized proton magnetic resonance spectroscopy.
Topics: Aspartic Acid; Autistic Disorder; Brain; Child; Child, Preschool; Choline; Creatine; Female; Humans; Intellectual Disability; Magnetic Resonance Spectroscopy; Male | 1997 |
Regional age dependence of human brain metabolites from infancy to adulthood as detected by quantitative localized proton MRS.
Topics: Adolescent; Age Factors; Aspartic Acid; Basal Ganglia; Brain; Brain Neoplasms; Cerebellum; Child; Child, Preschool; Choline; Creatine; Epilepsies, Partial; Humans; Infant; Infant, Newborn; Inositol; Intellectual Disability; Intracranial Arteriovenous Malformations; Magnetic Resonance Spectroscopy; Movement Disorders; Thalamus; Tissue Distribution | 1999 |
Treatment of pyruvate carboxylase deficiency with high doses of citrate and aspartate.
Topics: Amino Acids; Aspartic Acid; Child, Preschool; Citric Acid; Dose-Response Relationship, Drug; Female; Follow-Up Studies; Humans; Infant; Intellectual Disability; Ketosis; Lactic Acid; Pyruvate Carboxylase Deficiency Disease; Treatment Outcome | 1999 |
Mental retardation and behavioral problems as presenting signs of a creatine synthesis defect.
Topics: Aspartic Acid; Body Fluids; Brain Diseases, Metabolic; Child, Preschool; Creatine; Diagnosis, Differential; Epilepsy; Follow-Up Studies; Glycine; Humans; Infant; Intellectual Disability; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Mental Disorders | 2000 |
Prefrontal and medial temporal correlates of repetitive violence to self and others.
Topics: Adult; Amygdala; Aspartic Acid; Choline; Female; Hippocampus; Humans; Intellectual Disability; Interpersonal Relations; Magnetic Resonance Spectroscopy; Male; Phosphocreatine; Prefrontal Cortex; Severity of Illness Index; Temporal Lobe; Violence | 2000 |
Alterations of amino acids and monoamine metabolism in male Fmr1 knockout mice: a putative animal model of the human fragile X mental retardation syndrome.
Topics: 3,4-Dihydroxyphenylacetic Acid; Aging; Alanine; Amino Acids; Animals; Aspartic Acid; Brain; Brain Stem; Cerebellum; Cerebral Cortex; Chromatography, High Pressure Liquid; Corpus Striatum; Dopamine; Fragile X Mental Retardation Protein; Fragile X Syndrome; gamma-Aminobutyric Acid; Glutamic Acid; Glutamine; Hippocampus; Homovanillic Acid; Hydroxyindoleacetic Acid; Intellectual Disability; Male; Mice; Mice, Knockout; Models, Animal; Nerve Tissue Proteins; RNA-Binding Proteins; Serotonin; Taurine; Thalamus | 2001 |
Aspartylglycosaminuria in Northern Norway in eight patients: clinical heterogeneity and variations with the diet.
Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Child, Preschool; Creatinine; Dietary Proteins; Female; Glucosamine; Humans; Intellectual Disability; Male; Mucolipidoses | 1978 |
Aspartylglycosaminuria, urinary excretion of aspartylglycosamines related to mental retardation.
Topics: Adolescent; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Child, Preschool; Glucosamine; Humans; Intellectual Disability; Mucolipidoses | 1978 |
Studies on N-aspartyl-beta-glucosaminidase in aspartylglycosaminuria.
Topics: Animals; Aspartic Acid; Carbohydrate Metabolism, Inborn Errors; Cell Nucleus; Chromatography, Agarose; Hexosamines; Hexosaminidases; Humans; Intellectual Disability; Liver; Lysosomes; Mitochondria, Liver; Rats; Subcellular Fractions | 1975 |
[Cri-du-chat disease: plasma and urinary amino acids].
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Asparagine; Aspartic Acid; Child; Child, Preschool; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosome Mapping; Chromosomes, Human, Pair 5; Cri-du-Chat Syndrome; Female; Histidine; Humans; Intellectual Disability; Male; Models, Biological; Purine-Pyrimidine Metabolism, Inborn Errors | 1990 |
Dicarboxylic aminoaciduria associated with mental retardation.
Topics: Amino Acids, Dicarboxylic; Aspartic Acid; Child; Female; Glutamates; Glutamic Acid; Humans; Intellectual Disability | 1989 |
Aspartame. Review of safety issues. Council on Scientific Affairs.
Topics: Adolescent; Adult; Animals; Aspartame; Aspartic Acid; Brain Chemistry; Brain Diseases; Brain Neoplasms; Carbonated Beverages; Carcinogens; Child; Dietary Carbohydrates; Diketopiperazines; Dipeptides; Drug Stability; Endocrine System Diseases; Female; Glutamates; Glutamic Acid; Humans; Infant; Intellectual Disability; Methanol; Mice; Neurotransmitter Agents; Phenylalanine; Phenylketonurias; Piperazines; Pregnancy; Rats | 1985 |
[Characteristics of the amino acid spectrum of the blood of children with intellectual deficiency].
Topics: Amino Acids; Ammonia; Arginine; Aspartic Acid; Child; Female; Glutamates; Glutamic Acid; Humans; Intellectual Disability; Male; Movement Disorders; Polyamines; Syndrome; Urea | 1986 |
N-acetylaspartic aciduria due to aspartoacylase deficiency--a new aetiology of childhood leukodystrophy.
Topics: Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Brain; Diffuse Cerebral Sclerosis of Schilder; Humans; Infant; Intellectual Disability; Male | 1987 |
Aspartylglycosaminuria. An inborn error of metabolism associated with mental defect.
Topics: Adult; Asparagine; Aspartic Acid; Female; Glucosamine; Glucosidases; Glycoproteins; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Oligosaccharides; Peptide Hydrolases | 1968 |
Aspartylglycosaminuria (AGU). Further aspects on its clinical picture, mode of inheritance and epidemiology based on a series of 57 patients.
Topics: Adolescent; Adult; Amidohydrolases; Aspartic Acid; Bone Marrow; Child; Child, Preschool; Consanguinity; Face; Female; Finland; Genes, Recessive; Glucosamine; Homozygote; Humans; Inclusion Bodies; Infant; Infant, Newborn; Intellectual Disability; Lymphocytes; Male; Metabolism, Inborn Errors; Osteochondritis; Radiography; Syndrome | 1973 |
[Use of a preparation with a base of L-citrulline and L-acetylaspartic acid in minors with "mental fatigue" and slight "mental retardation"].
Topics: Adolescent; Aspartic Acid; Child; Citrulline; Female; Humans; Intellectual Disability; Male; Mental Fatigue | 1966 |
A search for aspartylglycosaminuria in Poland.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Child, Institutionalized; Chromatography, Paper; Glycosuria; Humans; Intellectual Disability; Phenylketonurias; Poland | 1974 |
Glycoasparagines in the urine of patients with aspartylglycosaminuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Asparagine; Aspartic Acid; Chromatography; Chromatography, Ion Exchange; Fucose; Galactose; Humans; Hydrogen-Ion Concentration; Intellectual Disability; Molecular Weight | 1972 |
Further speculation on the pathogenesis of Leigh's encephalomyelopathy.
Topics: Aspartic Acid; Brain Stem; Citric Acid Cycle; Encephalomalacia; Humans; Intellectual Disability; Ligases; Metabolism, Inborn Errors; Psychomotor Disorders; Syndrome; Thiamine | 1973 |
Medical research council unit for metabolic studies in psychiatry, Sheffield.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Bipolar Disorder; Catatonia; Circadian Rhythm; Cysteine; Humans; Intellectual Disability; Lithium; Mass Spectrometry; Mental Disorders; Metabolism, Inborn Errors; Periodicity; Phenylketonurias; Sleep; Vasopressins | 1973 |
Picture of the Month. Aspartylglucosaminuria.
Topics: Adolescent; Aspartic Acid; Body Height; Child; Child, Preschool; Chromatography, Thin Layer; Chromosome Aberrations; Chromosome Disorders; Electrophoresis; Face; Female; Finland; Genes, Recessive; Glucosamine; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors | 1974 |
Abnormal levels of aspartic acid, serine and cystine in the plasma in three cases of Rubinstein Taybi's syndrome.
Topics: Abnormalities, Multiple; Aspartic Acid; Chromatography, Ion Exchange; Cystine; Female; Humans; Intellectual Disability; Rubinstein-Taybi Syndrome; Serine | 1972 |
[Aspartylglucosaminuria].
Topics: Adolescent; Adult; Amidohydrolases; Aspartic Acid; Child; Child, Preschool; Female; Glucosamine; Humans; Infant; Intellectual Disability; Lysosomes; Male; Metabolism, Inborn Errors | 1972 |
[Amino acid excretion in urine and enzyme activities in blood of persons from 3 families with mental deficiency].
Topics: Acid Phosphatase; Adolescent; Adult; Alanine; Alkaline Phosphatase; Amino Acids; Aspartate Aminotransferases; Aspartic Acid; Chromatography, Thin Layer; Enzymes; Erythrocytes; Female; Glucosephosphate Dehydrogenase; Glutamates; Glycine; Humans; Intellectual Disability; L-Lactate Dehydrogenase; Leukocytes; Male; Middle Aged; Pedigree; Phenylalanine; Spectrophotometry; Tyrosine | 1969 |
Eleven new cases of aspartylglucosaminuria.
Topics: Abnormalities, Multiple; Acetamides; Adolescent; Adult; Aspartic Acid; Chromatography; Electroencephalography; Female; Glycosuria; Humans; Hyperkinesis; Intellectual Disability; Lymphocytes; Male; Metabolism, Inborn Errors | 1970 |
Detection of argininosuccinic aciduria by gas chromatography.
Topics: Arginine; Aspartic Acid; Ataxia; Chemical Precipitation; Chromatography, Gas; Epilepsy; Esters; Humans; Hydrogen-Ion Concentration; Intellectual Disability; Liver Diseases; Metabolism, Inborn Errors; Methods; Ornithine; Spectrum Analysis; Succinates | 1969 |
Metabolic traits in mentally retarded children as compared with normal populations: monoaminodicarboxylic acids and their half amides and total amino acids.
Topics: Adolescent; Alanine; Amino Acids; Arginine; Asparagine; Aspartic Acid; Child; Child, Preschool; Chromatography; Chromatography, Paper; Female; Glutamates; Glutamine; Glycine; Humans; Intellectual Disability; Male | 1969 |
Enzymatic cleavage of 2-acetamido-1-(beta'-L-aspartamido)-1,2-dideoxy-beta-D-glucose by human plasma and seminal fluid. Failure to detect the heterozygous state for aspartylglycosaminuria.
Topics: Amides; Aspartic Acid; Carbohydrates; Chromatography, Gel; Chromatography, Ion Exchange; Dextrans; Enzymes; Female; Glycoproteins; Heterozygote; Hexosamines; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Methods; Semen | 1969 |
Argininosuccinic aciduria: clinical, biochemical, anatomical and neuropathological observations.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Arginine; Aspartic Acid; Brain; Cerebellum; Citrulline; Female; Humans; Infant; Intellectual Disability; Liver; Lyases; Myelin Sheath; Neuroglia; Succinates | 1969 |